JP2012158599A - Synthesis of pyrrole-2-carbonitrile - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a method for the production of pyrrole-2-carbonitriles such as 1-methylpyrrole-2-carbonifirile.SOLUTION: The method preferably includes the steps of: reacting a pyrrole with chlorosulfonyl isocyanate in the presence of a solvent; and contacting the resulting product with a molar excess of an amide such as N,N-dimethylformamide. The product of this contacting step is then contacted with a molar excess of an organic base to produce a precipitate and a solution phase. The precipitate is then separated from the solution phase, and the corresponding pyrrole-2-carbonitrile is isolated from the resulting solution phase.

Description

CROSS REFERENCE TO RELATED APPLICATIONS This application claims the priority of US Patent Application No. 60 / 557,807 (filed 30 March 2004), the entire disclosure of which is hereby incorporated by reference. To do. This application is a U.S. patent application filed on March 25, 2005. Corresponding to

  The present invention is in the field of synthesis and isolation of pyrrole-2-carbonitrile, such as 1-methylpyrrole-2-carbonitrile.

  Pyrrole-2-carbonitrile is useful as an intermediate in the manufacture of compounds including pharmaceutical and insecticidal compositions. For example, see Patent Document 1 (related to thrombin inhibitor) and Patent Document 2 (related to pyrrole carbonitrile insecticide, acaricide, molluscicide).

  Non-Patent Document 1 suggests a method for synthesizing 1-methylpyrrole-2-carbonitrile, which includes the reaction of 1-methylpyrrole with chlorosulfonyl isocyanate in dichloromethane in the first step. In the method of Non-Patent Document 1, the product of the first step was reacted with DMF, and the reaction mixture was then poured into ice-cooled 4M HCL. After finishing the product and vacuum distillation, 1-methylpyrrole-2-carbonitrile was obtained in 58% yield.

Another method for synthesizing 1-methylpyrrole-2-carbonitrile from 1-methylpyrrole is to react with methanolic cyanide solution under anodizing conditions (Non-patent Document 2), in the presence of methanolic cyanide solution. Reacting with an excess of 1,4-dicyanobenzene as a sensitizer (Non-patent Document 3), and reacting trimethylsilylcyanide at -70 ° C. in tetraphenylformine-sensitized photooxidation (Non-patent Document 4). ), And reacting with newly prepared Ph ₃ P (SCN) ₂ at −40 ° C. (Non-patent Document 5). Another synthesis method starts from 2-pyrrolecarboxaldehyde (Non-patent document 6 and Non-patent document 7). Yet another method uses 2-pyrrolecarboxaldehyde as a starting material (Non-patent Documents 8 and 9). Such methods often require time consuming aqueous finishing and repeated extraction with ether, methylene chloride, or other suitable solvent. Some methods require the use of chromatography in the isolation / production process.

US Pat. No. 6,492,402 US Pat. No. 5,204,332

Barnett et al. Can. Chem. 1980, 58, 409 J. et al. Am. Chem. Soc. 1977, 99, 6111 J. et al. Chem. Soc. , Chem. Commun. 1978, 1108 J. et al. Am. Chem. Soc. 1985, 107, 5279 J. et al. Chem. Soc. Perkin Trans. I 1980, 1132 Can. J. et al. Chem. 1959, 37, 2053 J. et al. Chem. Soc. , Chem. Commun. 1972, 1226 J. et al. Prakt. Chem. 1994, 336, 467 Tetrahedron Lett. 1993, 34, 141

  In some embodiments, the present invention relates to a process for producing pyrrole-2-carbonitrile, such as 1-methylpyrrole-2-carbonitrile. Pyrrole is reacted with chlorosulfonyl isocyanate in the presence of a solvent that is substantially non-reactive with chlorosulfonyl isocyanate, and the resulting product is in a molar excess (preferably at least about 2.0 molar equivalents) of N , N-dialkylformamide. This product is then contacted with a molar excess (preferably at least about 2.0 molar equivalents) of organic base to obtain a precipitate and solution phase. The precipitate is then separated from the solution phase and the corresponding pyrrole-2-carbonitrile is isolated from the resulting solution phase. In some embodiments, water is added to the solution phase prior to isolation of pyrrole-2-carbonitrile. In certain embodiments, pyrrole-2-carbonitrile is isolated by distillation.

  In some embodiments, the solvent is toluene or acetonitrile. In some of these embodiments, it is preferred that the solvent comprises toluene.

  In another preferred embodiment, the N, N-dialkylformamide is N, N-dimethylformamide (DMF).

  In certain embodiments, the base is a tertiary amine or an aromatic amine. In some preferred embodiments, the base is triethylamine.

  In yet another embodiment, the reaction of pyrrole and chlorosulfonyl isocyanate is performed at a temperature of about 0 ° C. or less. In certain embodiments, 0.1 to 0.4 molar equivalents of water are added per equivalent of solvent to effect dilution. In certain preferred embodiments, the isolated solution phase is concentrated, then diluted and distilled.

  In another aspect, the invention also relates to the product produced by the method of the invention.

  The present invention relates to a process for producing pyrrole-2-carbonitrile, in particular 1-methylpyrrole-2-carbonitrile, preferably with improved isolated yield. In a preferred embodiment, the method of the present invention comprises reacting pyrrole, such as 1-methylpyrrole, with chlorosulfonyl isocyanate. In certain embodiments, the molar ratio of pyrrole to chlorosulfonyl isocyanate is from about 0.9: 1 to about 1.1: 1, preferably about 1: 1. It is also preferred that the reaction is conducted at about 0 ° C. or less. The product of this reaction is then contacted with N, N-dialkylformamide followed by the addition of an organic base.

Synthesis of 1-methylpyrrole-2-carbonitrile from 1-methylpyrrole is illustrated in Scheme 1 below.

While we do not intend to be bound by any particular theory or mechanism of operation, N, N-dialkylformamide (eg, N, N-dimethylformamide (DMF)) serves as a catalyst for the reaction. I think that. Two equivalents of DMF are preferably used in this process. During the reaction, it is believed that DMF · HCl and DMF · SO ₃ complexes are formed. It is believed that the use of a molar excess of DMF (preferably at least 2 equivalents) can avoid the release of gaseous by-products HCl and SO ₃ .

  Alkyl groups in N, N-dialkylformamide include, but are not limited to, aliphatic hydrocarbon chains having 1 to 6, preferably 1 to 4, more preferably 1 to 3 carbon atoms, Linear and branched chains such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, t-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, and isohexyl are included. N, N-dialkylformamides also include cyclic compositions, such as those in which the cyclic group may have 5-7, such as 6-membered ring components, such as N-formylpiperidine and N-formylmorpholine.

  Organic bases useful in the present invention include, but are not limited to, tertiary amines and aromatic amines. Tertiary amines include, but are not limited to, trimethylamine, triethylamine, tripropylamine, 1-methylpiperidine, 1,4-dimethylpiperazine, and N, N-diisopropylethylamine (Hunig's base). Aromatic amines include, but are not limited to, pyridine, 2-picoline, 2,6-lutidine, quinoline, 5,6,7,8-tetrahydroquinoline. In some embodiments, triethylamine is preferred.

  Solvents useful in the present invention are substantially non-reactive with chlorosulfonyl isocyanate. These solvents include aliphatic hydrocarbons (eg heptane), aromatic hydrocarbons (eg toluene), chlorinated hydrocarbons (eg methylene chloride), chlorobenzene, dialkyl ethers (eg diisopropyl ether) and alkyl nitriles ( For example, acetonitrile). In some embodiments, toluene or acetonitrile is preferred. In other embodiments, toluene is preferred.

The pyrrole moiety is generally sensitive to acids and will form tars in the presence thereof. In the process of the present invention, a molar excess of base, such as triethylamine (Et ₃ N) (preferably at least 2 equivalents), can be removed by filtration, a relatively pure solid salt (eg Et ₃ N · SO ₃ ) is believed to precipitate. The filtrate (eg containing Et ₃ N · HCl) can be worked up by water extraction. Applicants have reported that by triethylamine treatment, Barnett et al., J. MoI. Can. Chem. It was found that the 31-41% yield reported by 1980, 58, 409 increased to 65-76%.

  Applicants can distill the solution phase isolated after treatment with an organic base, but in some embodiments it is first possible to add at least some water, especially if the distillation is carried out at atmospheric pressure. I found it preferable to Without wishing to be limited by theory, it is believed that the addition of water destroys, for example, the toluene-nitrile complex. It has been found that the addition of water makes it possible to separate toluene from the product at temperatures below 85 ° C. In certain embodiments, 0.1-0.4 molar equivalents of water are used per equivalent of solvent.

  The invention is further illustrated by the following examples of preferred embodiments, which are described only for purposes of illustration and comparison with existing techniques, and unless otherwise indicated, the invention. It is understood that it is not intended to limit the scope of

  To a 5 liter flask was added acetonitrile (2.0 L) and 1-methylpyrrole (83 g, 3.5 mol). Chlorosulfonyl isocyanate (495 g, 3.5 mol) was added dropwise while maintaining a reaction temperature of −6 to 0 ° C. It should be noted that chlorosulfonyl isocyanate is corrosive and reacts violently with water. After stirring for 15 minutes, N, N-dimethylformamide (DMF, 511 g, 7.0 mol) was added at −4 to 0 ° C., followed by triethylamine (707 g, 7.0 mol) and stirring at 0 ° C. Continued with. The resulting white precipitate was filtered and washed with acetonitrile (200 mL). The filtrate was concentrated under reduced pressure. Water (4.0 L) was added to the residue, the phases were separated, and the aqueous phase was extracted with ethyl acetate (2 × 200 mL). The combined organic phases were washed with brine (3 × 500 mL). The organic phase was concentrated under reduced pressure and the residue was distilled using a Vigreux column at about 4 mm Hg / 70 ± 10 ° C. to give 1-methylpyrrole-2-carbonitrile (282 g, 76% yield). .

  The reaction was carried out in a manner generally similar to Example 1 except that 47.0 g of 1-methylpyrrole was substituted for acetonitrile with toluene. Two layers were formed after the addition of chlorosulfonyl isocyanate. Upon cooling to 0-5 ° C, the bottom layer solidified. The hygroscopic solid was collected by filtration and washed with toluene. The filtrate was concentrated to give 325 mL of a toluene solution (58.3 g, 95% yield) containing 0.55 mol of 1-methylpyrrole-2-carbonitrile (determined by 1H NMR).

  A crude solution of 1-methylpyrrole-2-carbonitrile in toluene prepared as in Example 2 in toluene was washed with brine containing sodium hydroxide to remove traces of acid. The separated organic layer (673 g) was subjected to atmospheric distillation (head temperature 110 to 115 ° C.) to remove most of the toluene. Water was added (total 255 mL) and distillation continued until the head temperature began to rise above 86 ° C. The pot residue (290 g) containing some water was fractionally distilled under reduced pressure to give 1-methylpyrrole-2-carbonitrile (217 g).

  All patent applications and other publications found in this application are incorporated herein by reference in their entirety.

Claims (18)

A process for preparing pyrrole-2-carbonitrile, comprising:
(A) reacting pyrrole with chlorosulfonyl isocyanate in the presence of a solvent;
(B) contacting the product of step (a) with a molar excess of N, N-dialkylformamide;
(C) contacting the product of step (b) with a molar excess of organic base, resulting in the formation of a precipitate and solution phase;
(D) separating the precipitate from the solution phase;
(E) A process comprising isolating pyrrole-2-carbonitrile from the solution phase of step (d).   The process of claim 1, wherein at least about 2.0 molar equivalents of N, N-dialkylformamide is used in step (b).   The method according to claim 1, wherein the organic base is a tertiary amine or an aromatic amine.   The method of claim 3, wherein at least about 2.0 molar equivalents of tertiary amine or aromatic amine is used in step (c).   The process according to any one of claims 1 to 4, wherein the pyrrole-2-carbonitrile is isolated by distillation. The method according to any one of claims 1 to 5, wherein the pyrrole is 1-methylpyrrole.   The method according to any one of claims 1 to 6, wherein the solvent is toluene or acetonitrile.   The method according to any one of claims 1 to 6, wherein the solvent is toluene.   The method according to any one of claims 3 to 8, wherein the tertiary amine is triethylamine.   The method according to any one of claims 3 to 8, wherein the aromatic amine is pyridine.   The method according to any one of claims 1 to 10, wherein the N, N-dialkylformamide is N, N-dimethylformamide, N-formylpiperidine, or N-formylmorpholine.   The method according to any one of claims 1 to 10, wherein the N, N-dialkylformamide is N, N-dimethylformamide.   The method according to any one of claims 1 to 12, wherein the molar ratio of pyrrole to chlorosulfonyl isocyanate is 0.9: 1 to 1.1: 1.   6. The process of claim 5, wherein water is added to the solution phase before distilling the pyrrole-2-carbonitrile from the solution phase of step (d).   15. A process according to claim 14, wherein from 0.1 to 0.4 molar equivalent of water is used per equivalent of solvent.   The process of claim 15, wherein the solution phase of step (d) is concentrated prior to the addition of water in step (e).   The method according to any one of claims 1 to 16, wherein step (a) is performed at a temperature of about 0 ° C or less.   A product produced by the method of any one of claims 1-17.